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Muscle & Nerve|March 1, 1988
Detection of muscle injury in humans with 31-P magnetic resonance spectroscopyK K McCully, Z Argov, B P Boden, et al.Neurologic Clinics|August 1, 1990
Mitochondrial encephalomyopathiesS DiMauro, E Bonilla, A Lombes, et al.Kidney International|May 1, 1994
Mitochondrial DNA deletion: a cause of chronic tubulointerstitial nephropathyM J Szabolcs, R Seigle, S Shanske, et al.Brain Pathology (Zurich, Switzerland)|April 1, 1992
Disorders associated with depletion of mitochondrial DNAE Ricci, C T Moraes, S Servidei, et al.Journal of Child Neurology|September 17, 1999
A novel mutation in the mitochondrial DNA transfer ribonucleic acidAsp gene in a child with myoclonic epilepsy and psychomotor regressionA Shtilbans, M El-Schahawi, E Malkin, et al.Biology of the Neonate|January 1, 1995
End-tidal carbon monoxide in newborn infants: observations during the 1st week of lifeV Balaraman, S Pelke, S DiMauro, et al.Neurology|April 1, 1993
Polyglucosan body disease simulating amyotrophic lateral sclerosisT D McDonald, P L Faust, C Bruno, et al.Neurology|August 10, 2005
Mitochondrial DNA copy number threshold in mtDNA depletion myopathyS E Durham, E Bonilla, D C Samuels, et al.Archives of Neurology|December 11, 1999
Mother with amyotrophic lateral sclerosis and daughter with Creutzfeldt-Jakob diseaseB B Worrall, L P Rowland, M Del Bene, et al.Annals of Neurology|October 1, 1985
Treatment of cerebrotendinous xanthomatosis with chenodeoxycholic acidT A Pedley, R G Emerson, C L Warner, et al.Pageof 44